197 Poster Multimodal, <strong>Chemosensory</strong> Measurement,Psychophysical, Clinical Olfactory, and TrigeminalODOR AND LATERALIZATION THRESHOLDS FORAMMONIA: A COMPARISON ACROSS STATIC ANDDYNAMIC OLFACTOMETRYSmeets M. 1 , Bulsing P. 1 , Ogink N. 2 , Van Thriel C. 3 , Dalton P. 4 1 UtrechtUniv, Utrecht, Netherlands; 2 A&F, Wageningen, Netherlands; 3 IFADO,Dortmund, Germany; 4 Monell Chemical Senses Center, Philadelphia,PALateralization thresholds (LT), in which irritancy is assessed by theability to localize to the stimulated nostril, have been used in the indoorair field in the context of setting occupational exposure limits. LT´s aretypically obtained using bottles (static olfactometry: SO) with singlechemical compound stimuli. However, if we wish to asses irritancy forcomplex mixtures, dynamic olfactometry (DO), in which odors arediluted in a clean air stream would be more appropriate. To this end, wecompared the performance of both methods using a single chemical,ammonia (NH3). Methods: Odor detection thresholds (ODT) and LT´sfor NH3 were collected using SO and DO (see above). A twoalternativeforced choice procedure was employed. 22 Females weretested on each method twice in a within-subjects design. Results: Forthe SO method, the (geometric) mean ODT = 2 (sem = 1.7), and LT =31 (sem = 1.3) ppm. For the DO method, the mean ODT = 2 (sem =1.2), and LT = 50 (sem = 1.3) ppm. There was no significant differencebetween methods (F < 1.0). Test-retest reliability was reasonable tohigh within methods (0.18 < r < 0.59) but low between methods (-0.09< r < 0.23). LT´s were significantly higher than ODT´s (p < 0.0001),thresholds measured at T=1 higher than at T=2 (p < 0.05). Conclusion:Both methods yielded very comparable mean results, and thus can beused interchangeably for estimates at the population level. However, onthe individual level, results should not be compared across methods.Funded by NWO 452-03-334198 Poster Multimodal, <strong>Chemosensory</strong> Measurement,Psychophysical, Clinical Olfactory, and TrigeminalIRRITATION, AMMONIA AND ASTHMAPetrova M. 1 , Diamond J. 1 , Schuster B.H. 2 , Dalton P. 1 1 Monell ChemicalSenses Center, Philadelphia, PA; 2 University of Dresden, Dresden,GermanySensitive subpopulations, such as those with asthma and otherrespiratory diseases, commonly attribute the exacerbation of asthmaticsymptoms to exposure to chemical odors and irritants. However, manyof the odors reported to cause asthma symptoms do not necessarilyreach concentrations capable of stimulating irritant receptors. The goalof the present study was to evaluate the irritation potential of ammonia(NH 3 ), and to determine whether there are any differences in nasal orocular irritant sensitivity between healthy individuals and those withmild-moderate asthma. 25 healthy and 15 mild-moderate asthmaticvolunteers (age 29.7 ± 10.8) were evaluated for their ability to detectodor and irritancy of NH 3 . Ammonia vapor was delivered to either sideof a set of specially-configured goggles (for the ocular exposure) or toeither nostril or both simultaneously for durations of 10 sec for thethresholds and up to 30 sec for the suprathreshold exposures.Additionally, 13 healthy and all asthmatic volunteers were evaluatedthroughout the testing sessions for pulmonary function usingspirometry. There were no significant differences in the sensoryirritation thresholds or rated intensity of irritation between asthmaticsubjects and healthy controls. Exposure to NH 3 didn´t alter pulmonaryfunction in either group. However, asthmatic individuals exhibitedsignificantly lower odor detection thresholds (93.24 ± 13.99 ppm,asthmatic, 153.35 ± 25.64 ppm healthy, P < 0.09). This implies that, insome instances, an adverse response to volatile chemicals amongasthmatics may be triggered by the perception of low-level odor, notirritation, and may reflect a psychogenically-mediated symptomresponse to a perceived health risk. Supported by NIH DC 03704 to PD.199 Poster Multimodal, <strong>Chemosensory</strong> Measurement,Psychophysical, Clinical Olfactory, and TrigeminalBREATHING RESPONSES OF NORMOSMIC AND ANOSMICINDIVIDUALS TO STIMULI PRESENTED IN ANENVIRONMENTAL CHAMBERWalker J.C. 1 , Walker D.B. 1 1 Sensory Research Institute, Florida StateUniversity, Tallahassee, FLTo investigate the effects of airborne contaminant exposures onbreathing in humans, we exposed 20 normosmics and 4 anosmics to 8conditions, each presented in 100-min sessions conducted in a 10m 3environmental chamber: environmental tobacco smoke (ETS) - 0, 15,100 and 800 µg/m 3 RSP; propionic acid (PA) - 0, 1, 10 and 15 ppm.Except with 15 ppm PA, for which the exposure plateau ended at min30, concentrations rose mins 11-20, were maintained through min 70and then declined. With normosmics, all PA concentrations caused amodest increase in inhalation duration (InDur). With the two lowest PAconcentrations, inhalation volume (InVol) was maintained whereas thisparameter declined slightly with 15 ppm PA and even more with cleanair. Thus, minute ventilation (MnVnt) was maintained over the courseof the session with 1 and 10 ppm PA while this parameter declined withclean air and, to a slightly less extent, with 15 ppm PA. With anosmicssmall increases and decreases, respectively, in InVol were seen with 1and 15 ppm PA. In normosmics, ETS increased InDur and decreasedInVol, resulting in a drop in MnVnt. Effects of ETS on anosmics werequite different. InDur was unchanged but InVol increased, with themagnitude of change following the order: 15>800>100 µg/m 3 . In theabsence of an InDur effect, the InVol pattern was repeated with theMnVnt parameter. This work will contribute to an improvedunderstanding of the principles underlying the integration ofchemosensory inputs, including ocular trigeminal, that yield changes inspecific breathing parameters under environmentally realisticconditions. Supported in part by the Philip Morris External ResearchProgram200 Poster Multimodal, <strong>Chemosensory</strong> Measurement,Psychophysical, Clinical Olfactory, and TrigeminalTEMPORAL INTEGRATION IN NASAL LATERALIZATIONOF ETHANOLWise P. 1 , Canty T. 1 , Wysocki C. 1 1 Monell Chemical Senses Center,Philadelphia, PATwo experiments examined how one can trade stimulus-duration withconcentration of n-ethyl alcohol to maintain a fixed level ofperformance in detection of nasal Irritation. Irritaiton threshold wasmeasured via nasal lateralization, a technique in which subjects receivechemical vapor in one nostril and clean air in the other. Subjects try todetermine which nostril received the chemical. Concentration was fixedwithin experimental runs, and stimulus-duration varied to find thebriefest stimulus subjects could reliably lateralize. Concentration variedbetween runs (1650 to 5000 ppm). Experiment 1 involved a small,intensively-tested group of subjects to obtain stable individual data.Experiment 2 involved a larger group and employed more rapidmethods. In both cases, a fixed-ratio increase in stimulus-duration couldcompensate for a fixed-ratio decrease in concentration. However, anincrease in duration of more the two-fold was required to compensatefor a two-fold decrease in concentration. These results suggest that asimple, but imperfect, mass-integrator model (i.e., an exponentiatedform of Haber´s rule) can describe short-term integration of nasallateralization of ethanol.50
201 Poster Multimodal, <strong>Chemosensory</strong> Measurement,Psychophysical, Clinical Olfactory, and TrigeminalPAIN INTENSITY RELATED CORTICAL ACTIVATIONFOLLOWING TRIGEMINAL STIMULATION OF THE NASALMUCOSA: FMRI STUDYWiesmann M. 1 , Kopietz R. 1 , Albrecht J. 1 , Schöpf V. 1 , Linn J. 1 ,Rzeznicka A. 1 , Anzinger A. 1 , Schreder T. 1 , Pollatos O. 1 , Kobal G. 21 Neuroradiology, University of Munich, Munich, Germany; 2 SensoryResearch R&T, Philip Morris USA Inc., Richmond, VAObjectives: The application of carbon dioxide (CO2) stimuli to thenasal mucosa is a well established model of acute experimentaltrigeminal pain. We studied the brain activation correlated with theintensity of painful trigeminal stimulation of the bilateral nasal mucosawithout concomittant tactile or thermal stimulation. Methods:Functional images following CO2-stimulation were obtained from 30healthy volunteers using a 1.5T MRI scanner (T2*-weighted EPIsequence, block-design). Images were analyzed using SPM2. Resultsand Conclusions: Following painful trigeminal stimulation, we foundactivation of brain areas known to be involved following chemicalstimulation of the nasal mucosa (orbitofrontal cortex), as well asassociation cortex (inferior, middle, and superior frontal gyri, superiorparietal lobule), and areas specific to the processing of painful andaversive stimuli (thalamus, S1, S2, amygdala). Cortical activationscorrelated with the intensity of the induced pain included anterior andmiddle cingulate gyrus, S2, thalamus, caudate nucleus, insula, andtrigeminal nuclei. Our data indicate that the experimental pain model ofCO2-stimulation of the nasal mucosa specifically activates thenociceptive cortex. The cortical network we found coding pain intensityis consistent with results from studies using peripheral pain models.Research described in this abstract was supported by Philip MorrisUSA Inc.202 Poster Multimodal, <strong>Chemosensory</strong> Measurement,Psychophysical, Clinical Olfactory, and TrigeminalEFFECTS OF IRRITANT CHEMICALS ON ORAL HEAT ANDCOLD PAIN PERCEPTIONAlbin K. 1 , Iodi Carstens M. 2 , Carstens E. 2 1 Food Science andTechnology, University of California, Davis, Davis, CA; 2 Neurobiology,Physiology and Behavior, University of California, Davis, Davis, CASome thermosensory transient receptor potential (TRP) channels alsorespond to common irritant chemicals. Capsaicin acts at the noxiousheat-sensitive TRPV1 channel, and menthol activates and enhancescold-evoked currents through TRPM8. We tested if irritants enhanceperceived hot and/or cold pain. One of the following was applied toone side of the tongue by filter paper: menthol (0.3%), capsaicin(0.001%), mustard oil (1%), or cinnamaldehyde (0.2%). The subjectthen pressed the tongue against a preheated Peltier thermode maintainedat 49°C or 9.5°C. In a 2-alternative forced choice (2-AFC) paradigm,subjects stated which side of the tongue had greater heat or cold pain,and then rated the intensity on each side, at 0, 1.5, 5, and 10 minutesafter chemical application. The method was validated by showing that~90% of subjects correctly identified a 0.5°C temperature difference.Capsaicin and mustard oil enhanced heat pain at 0, 1.5 and 5 min, as asignificant majority (p < 0.05, binomial test) chose the irritant-treatedside as more painful in the 2-AFC and assigned significantly higherintensity ratings to that side (p < 0.05, paired t-test). Cinnamaldehydeinitially enhanced heat pain. Neither capsaicin nor cinnamaldehydeaffected cold pain, while mustard oil significantly enhanced cold paininitially. Menthol significantly enhanced cold pain at 1.5 and 5 min butdid not affect heat pain. The results are consistent with the hypothesisthat capsaicin and menthol enhance thermal gating of TRPV1 andTRPM8, respectively, and additional experiments are underway tofurther test this.203 Poster Multimodal, <strong>Chemosensory</strong> Measurement,Psychophysical, Clinical Olfactory, and TrigeminalIS OVERALL TRIGEMINAL SENSITIVITY IMPAIRED INPATIENTS WITH OLFACTORY DYSFUNCTION?Frasnelli J. 1 , Schuster B. 2 , Lötsch J. 3 , Hummel T. 2 1 MontrealNeurological Institute, Mc Gill University, Montreal, Quebec, Canada;2 University of Dresden, Dresden, Germany; 3 Department ofPharmacology, pharmazentrum, Frankfurt a. M., GermanyTo investigate the relationship between cutaneous somatosensory andintranasal chemosensory trigeminal sensitivity, patients with olfactorydysfunction (n = 17 following URTI; n = 31 following head trauma)were tested and compared to 48 healthy controls. Trigeminalchemosensory function was tested using electrophysiological methods(negative mucosal potential—NMP; trigeminal event-relatedpotentials—tERP) and psychophysical techniques (lateralization task,CO2-thresholds). To test cutaneous somatosensory sensitivity, detectionthresholds and pain tolerance thresholds for electrical DC stimuli wereassessed unilaterally on the subjects´ cheeks. Patients had smaller tERPamplitudes and increased CO 2 -thresholds indicating decreasedchemosensory sensitivity (no difference for ratings and NMPamplitudes). In contrast, pain tolerance thresholds were lower inpatients indicating increased somatosensory sensitivity (no differencefor detection thresholds). As a conclusion, with regard to intranasalchemosensory measures, patients showed either decreased or similarsensitivity when compared to healthy controls. With regard tosomatosensory measures, however, they showed either similarsensitivity or higher responsiveness than healthy controls. This indicatesthat changes of trigeminal sensitivity in patients with olfactorydysfunction are specific to chemosensory sensations. Researchdescribed in this article was supported by Philip Morris USA Inc. andby Philip Morris International204 Poster Multimodal, <strong>Chemosensory</strong> Measurement,Psychophysical, Clinical Olfactory, and TrigeminalFEEL FROM SOLUBLE DUSTSCain W.S. 1 , Jalowayski A.A. 1 , Schmidt R. 1 , Kleinman M. 2 , WarrenC.B. 1 , Culver B. 3 1 Surgery (Otolaryngology), University of California,San Diego, La Jolla, CA; 2 Community and Environmental Medicine,University of California, Irvine, Irvine, CA; 3 Medicine (Epidemiology),University of California, Irvine, Irvine, CASubjects judged the feel of the soluble mineral dusts boric acid (2.5,5, 10 mg/m3), calcium oxide (2.5 mg/m3), and sodium borate[pentahydrate] (10 mg/m 3 ) during 47 min episodes of light exercise.The Ss indicated perceived sensory magnitude in the eyes, nose, andthroat by the concentration of carbon dioxide that matched thesensations. Consistent with previous work, the nose led with thehighest magnitude, followed by the throat, then the eyes. Perceivedmagnitude increased for periods up to 1/2 hr, then either held at aplateau or declined. This was true for all 3 agents, though with somedifferences in temporal signature. Accompanying measures impliedthat the decline of perceived magnitude in the nose occurred neitherbecause of an increase in dilution of the dissolved dusts in newlysecreted mucosal fluid nor from any increase of consequence in nasalresistance. Most likely, sensory adaptation principally determined thenon-monotonic change of increase then decrease over time. Theoutcome across agents showed, as expected, that calcium oxideexceeded sodium borate in potency. On the basis of mass exposure,boric acid behaved similarly to sodium borate, viz., the perceivedmagnitude of 10 mg/m 3 boric acid fell just slightly and insignificantlybelow 10 mg/m 3 sodium borate. Boric acid also showed a relatively flatdose-response relationship, i.e., a change in level caused only a smallchange in perceived magnitude. Supported by US Borax, Inc.51
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